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LABELS · 5b2d0f4e-5bba-4048-a2f0-bcb4b779efc0

Verzenio

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Preserved label snapshot, not confirmation of a current approved indication. Approval/withdrawal status must be checked for the exact disease, setting and regimen.

Label effective date
2026-07-13
Captured
2026-09-09T23:37:47.659725+00:00
Current indication reconciliation
Not reconciled

Indications and usage: exact source text

  1. 1 INDICATIONS AND USAGE VERZENIO ® is a kinase inhibitor indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence. ( 1.1 , 14.1 ) in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. ( 1.2 ) in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy. ( 1.2 ) as monotherapy for the treatment of adult patients with HR-positive, HER2-negative advanced or metastatic breast cancer with disease progression following endocrine therapy and prior chemotherapy in the metastatic setting. ( 1.2 ) 1.1 Early Breast Cancer VERZENIO ® (abemaciclib) is indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence [see Clinical Studies ( 14.1 )]. 1.2 Advanced or Metastatic Breast Cancer VERZENIO (abemaciclib) is indicated: in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy. as monotherapy for the treatment of adult patients with HR-positive, HER2-negative advanced or metastatic breast cancer with disease progression following endocrine therapy and prior chemotherapy in the metastatic setting.
Full extracted label fields
application numbers
  1. NDA208716
boxed warning exact
    brand names
    1. Verzenio
    current indication status
    not_reconciled
    dailymed set url
    https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=be4bc0de-0fdc-4d46-8d25-be43c79e6a06
    generic names
    1. ABEMACICLIB
    id
    5b2d0f4e-5bba-4048-a2f0-bcb4b779efc0
    indications and usage exact
    1. 1 INDICATIONS AND USAGE VERZENIO ® is a kinase inhibitor indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence. ( 1.1 , 14.1 ) in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. ( 1.2 ) in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy. ( 1.2 ) as monotherapy for the treatment of adult patients with HR-positive, HER2-negative advanced or metastatic breast cancer with disease progression following endocrine therapy and prior chemotherapy in the metastatic setting. ( 1.2 ) 1.1 Early Breast Cancer VERZENIO ® (abemaciclib) is indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence [see Clinical Studies ( 14.1 )]. 1.2 Advanced or Metastatic Breast Cancer VERZENIO (abemaciclib) is indicated: in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy. as monotherapy for the treatment of adult patients with HR-positive, HER2-negative advanced or metastatic breast cancer with disease progression following endocrine therapy and prior chemotherapy in the metastatic setting.
    indications and usage tables exact
      is original packager
      1. true
      manufacturer names
      1. Eli Lilly and Company
      matched search terms
      1. cancer
      package ndcs
      1. 0002-4483-54
      2. 0002-4483-62
      3. 0002-4815-54
      4. 0002-4815-62
      5. 0002-5337-54
      6. 0002-5337-63
      7. 0002-5337-62
      8. 0002-6216-54
      product ndcs
      1. 0002-4483
      2. 0002-4815
      3. 0002-5337
      4. 0002-6216
      product types
      1. HUMAN PRESCRIPTION DRUG
      recent major changes exact
        record type
        complete_spl_indications_section_candidate
        routes
        1. ORAL
        rxcuis
        1. 1946830
        2. 1946836
        3. 1946838
        4. 1946840
        5. 1946842
        6. 1946844
        7. 1946846
        8. 1946848
        source batch
        file
        /private/tmp/cancer-full-research/indications/raw/labels-00300.json
        meta
        disclaimer
        Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.
        last updated
        2026-09-09
        results
        limit
        100
        skip
        300
        total
        830
        sha256
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        url
        https://api.fda.gov/drug/label.json?search=%28indications_and_usage%3Acancer+OR+indications_and_usage%3Acarcinoma+OR+indications_and_usage%3Acarcinomas+OR+indications_and_usage%3Alymphoma+OR+indications_and_usage%3Alymphomas+OR+indications_and_usage%3Aleukemia+OR+indications_and_usage%3Aleukaemia+OR+indications_and_usage%3Asarcoma+OR+indications_and_usage%3Asarcomas+OR+indications_and_usage%3Amelanoma+OR+indications_and_usage%3Amyeloma+OR+indications_and_usage%3Atumor+OR+indications_and_usage%3Atumors+OR+indications_and_usage%3Atumour+OR+indications_and_usage%3Atumours+OR+indications_and_usage%3Aneoplasm+OR+indications_and_usage%3Aneoplasms+OR+indications_and_usage%3Amalignant+OR+indications_and_usage%3Amalignancy+OR+indications_and_usage%3Amyelodysplastic+OR+indications_and_usage%3Amyelofibrosis+OR+indications_and_usage%3Amastocytosis+OR+indications_and_usage%3Aglioma+OR+indications_and_usage%3Aglioblastoma+OR+indications_and_usage%3Aneuroblastoma+OR+indications_and_usage%3Aretinoblastoma+OR+indications_and_usage%3Apheochromocytoma+OR+indications_and_usage%3Aparaganglioma+OR+indications_and_usage%3Amyeloproliferative+OR+indications_and_usage%3Awaldenstrom+OR+indications_and_usage%3Apolycythemia+OR+indications_and_usage%3Athrombocythemia+OR+indications_and_usage%3Adesmoid+OR+indications_and_usage%3Aneurofibromatosis+OR+indications_and_usage%3Ahistiocytosis%29+AND+%28openfda.application_number%3ANDA%2A+OR+openfda.application_number%3ABLA%2A%29&limit=100&skip=300&sort=id%3Aasc
        source url
        https://api.fda.gov/drug/label.json?search=id%3A%225b2d0f4e-5bba-4048-a2f0-bcb4b779efc0%22
        spl effective date
        2026-07-13
        spl effective time
        20260713
        spl set id
        be4bc0de-0fdc-4d46-8d25-be43c79e6a06
        spl version
        30
        substance names
        1. ABEMACICLIB
        uniis
        1. 60UAB198HK
        verification flags
        1. oncology_keyword_candidate_not_clinically_classified
        2. spl_text_not_verified_identical_to_latest_approved_label
        3. individual_indications_not_split_or_reconciled
        4. fda_label_posted_after_spl_effective_date_requires_version_review
        Drugs@FDA application source records
        1. application number
          NDA208716
          payload
          all indexed label documents
          1. Appl No
            208716
            Application Docs Date
            2017-09-28 00:00:00
            Application Docs ID
            49872
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            1
            Submission Type
            ORIG
          2. Appl No
            208716
            Application Docs Date
            2018-08-21 00:00:00
            Application Docs ID
            55257
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            1
            Submission Type
            SUPPL
          3. Appl No
            208716
            Application Docs Date
            2019-09-11 00:00:00
            Application Docs ID
            59972
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            3
            Submission Type
            SUPPL
          4. Appl No
            208716
            Application Docs Date
            2020-03-31 00:00:00
            Application Docs ID
            62394
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            4
            Submission Type
            SUPPL
          5. Appl No
            208716
            Application Docs Date
            2021-10-13 00:00:00
            Application Docs ID
            68965
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            6
            Submission Type
            SUPPL
          6. Appl No
            208716
            Application Docs Date
            2021-10-13 00:00:00
            Application Docs ID
            68966
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            7
            Submission Type
            SUPPL
          7. Appl No
            208716
            Application Docs Date
            2021-10-13 00:00:00
            Application Docs ID
            68967
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            8
            Submission Type
            SUPPL
          8. Appl No
            208716
            Application Docs Date
            2023-03-03 00:00:00
            Application Docs ID
            73673
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            11
            Submission Type
            SUPPL
          9. Appl No
            208716
            Application Docs Date
            2023-03-03 00:00:00
            Application Docs ID
            73674
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            10
            Submission Type
            SUPPL
          10. Appl No
            208716
            Application Docs Date
            2024-11-14 00:00:00
            Application Docs ID
            80213
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            17
            Submission Type
            SUPPL
          11. Appl No
            208716
            Application Docs Date
            2025-03-03 00:00:00
            Application Docs ID
            81385
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            19
            Submission Type
            SUPPL
          12. Appl No
            208716
            Application Docs Date
            2026-07-15 00:00:00
            Application Docs ID
            86561
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            21
            Submission Type
            SUPPL
          all submission records
          1. Appl No
            208716
            Review Priority
            PRIORITY
            Submission Class Code ID
            7
            Submission No
            1
            Submission Status
            AP
            Submission Status Date
            2017-09-28 00:00:00
            Submission Type
            ORIG
            Submissions Public Notes
          2. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            3
            Submission No
            1
            Submission Status
            AP
            Submission Status Date
            2018-08-17 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          3. Appl No
            208716
            Review Priority
            901 REQUIRED
            Submission Class Code ID
            3
            Submission No
            3
            Submission Status
            AP
            Submission Status Date
            2019-09-09 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          4. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            2
            Submission No
            4
            Submission Status
            AP
            Submission Status Date
            2020-03-30 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          5. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            2
            Submission No
            6
            Submission Status
            AP
            Submission Status Date
            2021-10-12 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          6. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            2
            Submission No
            7
            Submission Status
            AP
            Submission Status Date
            2021-10-12 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          7. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            2
            Submission No
            8
            Submission Status
            AP
            Submission Status Date
            2021-10-12 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          8. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            2
            Submission No
            10
            Submission Status
            AP
            Submission Status Date
            2023-03-03 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          9. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            2
            Submission No
            11
            Submission Status
            AP
            Submission Status Date
            2023-03-03 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          10. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            2
            Submission No
            17
            Submission Status
            AP
            Submission Status Date
            2024-11-13 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          11. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            3
            Submission No
            19
            Submission Status
            AP
            Submission Status Date
            2025-02-27 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          12. Appl No
            208716
            Review Priority
            STANDARD
            Submission Class Code ID
            2
            Submission No
            21
            Submission Status
            AP
            Submission Status Date
            2026-07-13 00:00:00
            Submission Type
            SUPPL
            Submissions Public Notes
          application number
          NDA208716
          approval interpretation
          Application linkage and approved submission are not indication-level current approval verification
          current indication status
          not_reconciled
          has approved submission record
          true
          latest approved submission date
          2026-07-13
          latest label selection rule
          max FDA ApplicationDocsDate, including all ties; posting date is not approval date and latest indexed document may be incomplete
          latest posted label documents
          1. Appl No
            208716
            Application Docs Date
            2026-07-15 00:00:00
            Application Docs ID
            86561
            Application Docs Title
            0
            Application Docs Type ID
            2
            Submission No
            21
            Submission Type
            SUPPL
          official application record
          Appl No
          208716
          Appl Public Notes
          Appl Type
          NDA
          Sponsor Name
          ELI LILLY AND CO
          openfda application present
          true
          products
          1. Active Ingredient
            ABEMACICLIB
            Appl No
            208716
            Drug Name
            VERZENIO
            Form
            TABLET;ORAL
            Product No
            001
            Reference Drug
            1
            Reference Standard
            0
            Strength
            50MG
            marketing status
            1. Prescription
          2. Active Ingredient
            ABEMACICLIB
            Appl No
            208716
            Drug Name
            VERZENIO
            Form
            TABLET;ORAL
            Product No
            002
            Reference Drug
            1
            Reference Standard
            0
            Strength
            100MG
            marketing status
            1. Prescription
          3. Active Ingredient
            ABEMACICLIB
            Appl No
            208716
            Drug Name
            VERZENIO
            Form
            TABLET;ORAL
            Product No
            003
            Reference Drug
            1
            Reference Standard
            0
            Strength
            150MG
            marketing status
            1. Prescription
          4. Active Ingredient
            ABEMACICLIB
            Appl No
            208716
            Drug Name
            VERZENIO
            Form
            TABLET;ORAL
            Product No
            004
            Reference Drug
            1
            Reference Standard
            1
            Strength
            200MG
            marketing status
            1. Prescription

        Source passages and status connections

        Passage classifications are automated and are not treatment recommendations. Connections apply only to their recorded indication scope.

        Passage 1 · positive indication candidate
        application numbers
        1. NDA208716
        brand names
        1. Verzenio
        classification reasons
        1. explicit_positive_indication_predicate
        2. tumor_or_malignant_hematology_words_in_positive_statement
        3. positive_statement_also_contains_qualification_review_required
        clinical review status
        pending
        content role
        positive_indication_candidate
        context span
        end
        546
        end exclusive
        true
        exact text
        1 INDICATIONS AND USAGE VERZENIO ® is a kinase inhibitor indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence. ( 1.1 , 14.1 ) in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor rec
        label id
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        duplicate text group
        dup-78f6abb92959f73012bb
        extraction review status
        automated_candidate_pending_source_review
        generic names
        1. ABEMACICLIB
        id
        ind-span-a51797e23258b20301f2
        label id
        5b2d0f4e-5bba-4048-a2f0-bcb4b779efc0
        positive predicate support span
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        end exclusive
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        is a kinase inhibitor indicated
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        qualifier mentions
        1. context exact
          en or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth
          kind
          age
          polarity
          not_inferred
          span
          end
          188
          end exclusive
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          exact text
          adult patients
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          or (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurre
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          HER2)-negative
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        3. context exact
          crine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor
          kind
          stage_or_setting
          polarity
          not_inferred
          span
          end
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          exact text
          adjuvant treatment of adult patients with h
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        4. context exact
          TIONS AND USAGE VERZENIO ® is a kinase inhibitor indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early br
          kind
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          247
          end exclusive
          true
          exact text
          in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growt
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        regulatory links
          schema version
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          source defined aliases
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            exact text
            1 INDICATIONS AND USAGE VERZENIO ® is a kinase inhibitor indicated: in combination with endocrine therapy (tamoxifen or an aromatase inhibitor) for the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence.
            label id
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            offset unit
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            source array index
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            source field
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            source url
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            spl effective date
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            spl set id
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            spl version
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            structured fields status
            not_extracted_no_values_inferred_from_mentions
            structured indication
            age
            Source null
            approval pathway
            Source null
            biomarker and test
            Source null
            disease stage
            Source null
            limitations
            Source null
            line
            Source null
            prior therapy
            Source null
            regimen
            Source null
            tumor histology
            Source null
            use intent
            tumor_directed_candidate
            Passage 2 · positive indication candidate
            application numbers
            1. NDA208716
            brand names
            1. Verzenio
            classification reasons
            1. inherited_predicate_from_same_label_section_requires_review
            2. tumor_or_malignant_hematology_words_in_positive_statement
            clinical review status
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            content role
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            context span
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            true
            exact text
            the adjuvant treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative, node-positive, early breast cancer at high risk of recurrence. ( 1.1 , 14.1 ) in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. ( 1.2 ) in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast
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                                                  1.2 Advanced or Metastatic Breast Cancer VERZENIO (abemaciclib) is indicated: in combination with an aromatase inhibitor as initial endocrine-based therapy for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer. in combination with fulvestrant for the treatment of adult patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced or metastatic breast cancer with disease progression following endocrine therapy. as monotherapy for the treatment of adult patients with HR-positive, HER2-negative advanced or metastatic breast cancer with disease progression following endocrine therapy and prior chemotherapy in the metastatic setting.
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                                                  5b2d0f4e-5bba-4048-a2f0-bcb4b779efc0
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                                                  source url
                                                  https://api.fda.gov/drug/label.json?search=id%3A%225b2d0f4e-5bba-4048-a2f0-bcb4b779efc0%22
                                                  spl effective date
                                                  2026-07-13
                                                  spl set id
                                                  be4bc0de-0fdc-4d46-8d25-be43c79e6a06
                                                  spl version
                                                  30
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                                                  not_extracted_no_values_inferred_from_mentions
                                                  structured indication
                                                  age
                                                  Source null
                                                  approval pathway
                                                  Source null
                                                  biomarker and test
                                                  Source null
                                                  disease stage
                                                  Source null
                                                  limitations
                                                  Source null
                                                  line
                                                  Source null
                                                  prior therapy
                                                  Source null
                                                  regimen
                                                  Source null
                                                  tumor histology
                                                  Source null
                                                  use intent
                                                  tumor_directed_candidate

                                                  Preserved source evidence · Not medical advice